SU489354A3 - Способ крашени и набивки текстильных материалов - Google Patents
Способ крашени и набивки текстильных материаловInfo
- Publication number
 - SU489354A3 SU489354A3 SU1776272A SU1776272A SU489354A3 SU 489354 A3 SU489354 A3 SU 489354A3 SU 1776272 A SU1776272 A SU 1776272A SU 1776272 A SU1776272 A SU 1776272A SU 489354 A3 SU489354 A3 SU 489354A3
 - Authority
 - SU
 - USSR - Soviet Union
 - Prior art keywords
 - weight
 - dyeing
 - group
 - textile materials
 - cii
 - Prior art date
 
Links
- 239000000463 material Substances 0.000 title description 5
 - 238000004043 dyeing Methods 0.000 title description 4
 - 238000000034 method Methods 0.000 title description 3
 - 239000004753 textile Substances 0.000 title description 2
 - 239000000975 dye Substances 0.000 description 10
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
 - 125000003118 aryl group Chemical group 0.000 description 7
 - HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
 - 125000003710 aryl alkyl group Chemical group 0.000 description 5
 - 239000004744 fabric Substances 0.000 description 5
 - 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
 - -1 6-hydroxy-2-pyridoyl Chemical class 0.000 description 4
 - 125000003342 alkenyl group Chemical group 0.000 description 3
 - KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
 - 150000001875 compounds Chemical class 0.000 description 3
 - 238000005406 washing Methods 0.000 description 3
 - ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
 - QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
 - RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
 - 125000000217 alkyl group Chemical group 0.000 description 2
 - 150000001412 amines Chemical class 0.000 description 2
 - 125000000753 cycloalkyl group Chemical group 0.000 description 2
 - 238000001035 drying Methods 0.000 description 2
 - 239000000835 fiber Substances 0.000 description 2
 - 125000000623 heterocyclic group Chemical group 0.000 description 2
 - 230000007935 neutral effect Effects 0.000 description 2
 - 235000011121 sodium hydroxide Nutrition 0.000 description 2
 - 239000000126 substance Substances 0.000 description 2
 - 125000000547 substituted alkyl group Chemical group 0.000 description 2
 - QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
 - AJHPGXZOIAYYDW-UHFFFAOYSA-N 3-(2-cyanophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)NC(C(O)=O)CC1=CC=CC=C1C#N AJHPGXZOIAYYDW-UHFFFAOYSA-N 0.000 description 1
 - OCKGFTQIICXDQW-ZEQRLZLVSA-N 5-[(1r)-1-hydroxy-2-[4-[(2r)-2-hydroxy-2-(4-methyl-1-oxo-3h-2-benzofuran-5-yl)ethyl]piperazin-1-yl]ethyl]-4-methyl-3h-2-benzofuran-1-one Chemical compound C1=C2C(=O)OCC2=C(C)C([C@@H](O)CN2CCN(CC2)C[C@H](O)C2=CC=C3C(=O)OCC3=C2C)=C1 OCKGFTQIICXDQW-ZEQRLZLVSA-N 0.000 description 1
 - RXQNKKRGJJRMKD-UHFFFAOYSA-N 5-bromo-2-methylaniline Chemical compound CC1=CC=C(Br)C=C1N RXQNKKRGJJRMKD-UHFFFAOYSA-N 0.000 description 1
 - LPXQRXLUHJKZIE-UHFFFAOYSA-N 8-azaguanine Chemical compound NC1=NC(O)=C2NN=NC2=N1 LPXQRXLUHJKZIE-UHFFFAOYSA-N 0.000 description 1
 - 241001116389 Aloe Species 0.000 description 1
 - 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
 - 240000008886 Ceratonia siliqua Species 0.000 description 1
 - LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
 - 101100134922 Gallus gallus COR5 gene Proteins 0.000 description 1
 - UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
 - 239000002202 Polyethylene glycol Substances 0.000 description 1
 - 239000004793 Polystyrene Substances 0.000 description 1
 - VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
 - 229960000583 acetic acid Drugs 0.000 description 1
 - 239000002253 acid Substances 0.000 description 1
 - 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
 - 125000003545 alkoxy group Chemical group 0.000 description 1
 - 235000011399 aloe vera Nutrition 0.000 description 1
 - 229960004050 aminobenzoic acid Drugs 0.000 description 1
 - BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
 - 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
 - 235000011130 ammonium sulphate Nutrition 0.000 description 1
 - 239000007900 aqueous suspension Substances 0.000 description 1
 - 125000004429 atom Chemical group 0.000 description 1
 - 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
 - 239000000969 carrier Substances 0.000 description 1
 - 239000003086 colorant Substances 0.000 description 1
 - 230000008878 coupling Effects 0.000 description 1
 - 238000010168 coupling process Methods 0.000 description 1
 - 238000005859 coupling reaction Methods 0.000 description 1
 - 230000000779 depleting effect Effects 0.000 description 1
 - 150000002148 esters Chemical class 0.000 description 1
 - 235000013312 flour Nutrition 0.000 description 1
 - 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
 - 239000012362 glacial acetic acid Substances 0.000 description 1
 - 229910052736 halogen Inorganic materials 0.000 description 1
 - 150000002367 halogens Chemical class 0.000 description 1
 - 125000005842 heteroatom Chemical group 0.000 description 1
 - VEXZGXHMUGYJMC-UHFFFAOYSA-N hydrochloric acid Substances Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
 - 229910052739 hydrogen Inorganic materials 0.000 description 1
 - 239000001257 hydrogen Substances 0.000 description 1
 - NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
 - 239000000203 mixture Substances 0.000 description 1
 - 125000005429 oxyalkyl group Chemical group 0.000 description 1
 - 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
 - 229920002401 polyacrylamide Polymers 0.000 description 1
 - 229920000728 polyester Polymers 0.000 description 1
 - 229920001223 polyethylene glycol Polymers 0.000 description 1
 - 229920000139 polyethylene terephthalate Polymers 0.000 description 1
 - 239000005020 polyethylene terephthalate Substances 0.000 description 1
 - 229920002223 polystyrene Polymers 0.000 description 1
 - 239000000843 powder Substances 0.000 description 1
 - 230000005855 radiation Effects 0.000 description 1
 - 239000010802 sludge Substances 0.000 description 1
 - 239000000344 soap Substances 0.000 description 1
 - 239000001632 sodium acetate Substances 0.000 description 1
 - 235000017281 sodium acetate Nutrition 0.000 description 1
 - JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
 - LIBWRRJGKWQFSD-UHFFFAOYSA-M sodium;2-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC=C1S([O-])(=O)=O LIBWRRJGKWQFSD-UHFFFAOYSA-M 0.000 description 1
 - 238000010025 steaming Methods 0.000 description 1
 - 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
 - ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
 - C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
 - C09B29/00—Monoazo dyes prepared by diazotising and coupling
 - C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
 - C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
 - C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
 - C09B29/3617—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
 - C09B29/3621—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring
 - C09B29/3626—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O)
 - C09B29/363—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O) from diazotized amino carbocyclic rings
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Coloring (AREA)
 - Pyridine Compounds (AREA)
 - Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| DE19712120095 DE2120095A1 (de) | 1971-04-24 | 1971-04-24 | Wasserunlösliche Monoazofarbstoffe und Verfahren zu ihrer Herstellung | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| SU489354A3 true SU489354A3 (ru) | 1975-10-25 | 
Family
ID=5805799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| SU1776272A SU489354A3 (ru) | 1971-04-24 | 1972-04-21 | Способ крашени и набивки текстильных материалов | 
Country Status (15)
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| CH471861A (de) * | 1968-01-18 | 1969-04-30 | Sandoz Ag | Verfahren zur Herstellung von Monoazoverbindungen | 
| CH503781A (de) * | 1968-05-15 | 1971-02-28 | Sandoz Ag | Verfahren zur Herstellung von basischen Farbstoffen | 
| DE1917278B2 (de) * | 1969-04-03 | 1974-06-27 | Basf Ag, 6700 Ludwigshafen | Monoazofarbstoffe, Verfahren zu deren Herstellung und Farbstoffzubereitungen | 
- 
        1971
        
- 1971-04-24 DE DE19712120095 patent/DE2120095A1/de active Pending
 
 - 
        1972
        
- 1972-04-13 NL NL7204977A patent/NL7204977A/xx not_active Application Discontinuation
 - 1972-04-19 IT IT23410/72A patent/IT954842B/it active
 - 1972-04-20 BE BE782424A patent/BE782424A/xx unknown
 - 1972-04-20 BR BR2466/72A patent/BR7202466D0/pt unknown
 - 1972-04-20 DD DD162445A patent/DD105623A5/xx unknown
 - 1972-04-21 CA CA140,231A patent/CA958006A/en not_active Expired
 - 1972-04-21 FR FR7214181A patent/FR2134400B1/fr not_active Expired
 - 1972-04-21 AT AT353272A patent/AT309620B/de not_active IP Right Cessation
 - 1972-04-21 SU SU1776272A patent/SU489354A3/ru active
 - 1972-04-21 ZA ZA722696A patent/ZA722696B/xx unknown
 - 1972-04-21 AU AU41455/72A patent/AU468752B2/en not_active Expired
 - 1972-04-24 ES ES402044A patent/ES402044A1/es not_active Expired
 - 1972-04-24 CH CH604672A patent/CH566370A5/xx not_active IP Right Cessation
 - 1972-04-24 GB GB1883872A patent/GB1388701A/en not_active Expired
 
 
Also Published As
| Publication number | Publication date | 
|---|---|
| BE782424A (fr) | 1972-10-20 | 
| CA958006A (en) | 1974-11-19 | 
| AU468752B2 (en) | 1976-01-22 | 
| DE2120095A1 (de) | 1972-11-02 | 
| NL7204977A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1972-10-26 | 
| CH566370A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-09-15 | 
| AT309620B (de) | 1973-08-27 | 
| FR2134400A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1972-12-08 | 
| IT954842B (it) | 1973-09-15 | 
| ZA722696B (en) | 1973-02-28 | 
| ES402044A1 (es) | 1975-11-01 | 
| BR7202466D0 (pt) | 1973-06-12 | 
| DD105623A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-05-05 | 
| AU4145572A (en) | 1973-10-25 | 
| FR2134400B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-12-20 | 
| GB1388701A (en) | 1975-03-26 | 
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